Investigating the mechanism of chloroplast singlet oxygen signaling in the Arabidopsis thaliana accelerated cell death 2 mutant

ABSTRACT As sessile organisms, plants have evolved complex signaling mechanisms to sense stress and acclimate. This includes the use of reactive oxygen species (ROS) generated during dysfunctional photosynthesis to initiate signaling. One such ROS, singlet oxygen (1O2), can trigger retrograde signaling, chloroplast degradation, and programmed cell death. However, the signaling mechanisms are largely unknown. Several proteins (e.g. PUB4, OXI1, EX1) are proposed to play signaling roles across three Arabidopsis thaliana mutants that conditionally accumulate chloroplast 1O2 (fluorescent in blue light (flu), chlorina 1 (ch1), and plastid ferrochelatase 2 (fc2)). We previously demonstrated that these mutants reveal at least two chloroplast 1O2 signaling pathways (represented by flu and fc2/ch1). Here, we test if the 1O2-accumulating lesion mimic mutant, accelerated cell death 2 (acd2), also utilizes these pathways. The pub4–6 allele delayed lesion formation in acd2 and restored photosynthetic efficiency and biomass. Conversely, an oxi1 mutation had no measurable effect on these phenotypes. acd2 mutants were not sensitive to excess light (EL) stress, yet pub4–6 and oxi1 both conferred EL tolerance within the acd2 background, suggesting that EL-induced 1O2 signaling pathways are independent from spontaneous lesion formation. Thus, 1O2 signaling in acd2 may represent a third (partially overlapping) pathway to control cellular degradation.


Introduction
To thrive while rooted to the ground, plants have acquired the ability to sense changes in their environment and acclimate.While plants employ diverse mechanisms to achieve such plastic physiologies, it is clear that they can use their chloroplasts (photosynthetic plastid organelles) to sense and respond to multiple types of abiotic and biotic stresses.This is due, in part, to chloroplasts being the site of photosynthesis.Such high energy metabolism is prone to producing reactive oxygen species (ROS), particularly under stress conditions such as drought, excess light (EL), salinity, and pathogen attack, [1][2][3] While these ROS can be toxic and lead to the damage of macromolecules in the chloroplast, they also act as signaling molecules. 4One ROS in particular, singlet oxygen ( 1 O 2 ), is predominantly associated with chloroplasts (unlike superoxide and hydrogen peroxide (H 2 O 2 ), which are made in multiple cellular compartments) and produced primarily at photosystem II during photosynthesis due to excited triplet-state chlorophylls interacting with molecular oxygen, 5-7 1 O 2 is known to trigger changes in nuclear gene expression (e.g., retrograde signaling), 8,9 selective chloroplast degradation (i.e., chloroplast quality control), 10,11 and programmed cell death (PCD). 12,13Due to the extremely short halflife of 1 O 2 (<1 μsec, 14 the bulk of this ROS is expected to remain within the chloroplasts in which it is made, necessitating the existence of signaling cascades.However, how 1 O 2 triggers such signaling and leads to these effects predominantly remains an open question in plant cell biology. To study these signals, researchers have primarily relied on three Arabidopsis thaliana mutants that conditionally accumulate 1 O 2 in chloroplasts.The first characterized, fluorescent in blue light (flu), 15 accumulates the tetrapyrrole chlorophyll precursor protochlorophyllide (Pchlide) in the dark.Upon a shift to light, this photosensitizing molecule leads to a rapid burst of 1 O 2 within chloroplasts that initiates a signal from the grana margins, 16 which leads to retrograde signaling and PCD. 9,13 second mutant chlorina (ch1), cannot produce chlorophyll b, leaving the PSII reaction center without a protective antenna and sensitive to EL stress. 12Under EL, ch1 mutants produce a large amount of 1 O 2 at PSII within the grana core leading to retrograde signaling and PCD. 12,17This 1 O 2 can also lead to EL acclimation and increase EL tolerance, a process that requires METHYLENE BLUE SENSITIVITY 1 (MBS1) in Arabidopsis 18 and green algae. 19Finally, a third mutant, plastid ferrochelatase 2 (fc2), accumulates the chloroplast tetrapyrrole intermediate protoporphyrin IX (Proto) immediately after dawn. 10 Like Pchlide, free Proto also leads to the generation of 1 O 2 in the light, although the exact location of where the 1 O 2 is generated is unknown.
In all three mutants, the accumulation of chloroplast 1 O 2 leads to the induction of similar sets of nuclear marker genes, rapid bleaching of photosynthetic tissue, and eventual cell death. 9,10,12In the case of fc2, these signals also lead to selective 11 and wholesale chloroplast degradation, 10  are not due to the toxicity of 1 O 2 per se, but to a genetically programmed response to its accumulation.In all three mutants, genetic suppressors have been identified through forward and reverse genetic approaches and many of these suppressor mutations can block signaling without reducing 1 O 2 levels. 1 O 2 signaling in flu can be blocked by mutations in EXECUTOR1 (EX1) 13 and EX2 , 20 which encode two chloroplast thylakoid-localized proteins.Signaling in flu is also blocked by mutations in CRYTOCHROME1 (CRY1), 21 which encodes a nuclear-/cytoplasmic-localized blue light photoreceptor.In ch1, mutations affecting OXIDATIVE INDUCIBLE SIGNAL1 (OXI1) block 1 O 2 signaling. 17OXI1 is a nuclearlocalized Ser/Thr kinase, originally identified for its role in pathogen defense. 22Finally, several mutations that block 1 O 2 signaling in fc2 have been identified. 10,23,24One mutation, pub4-6, affects the E3 ubiquitin ligase Plant U-Box 4 (PUB4), which may be involved (directly or indirectly) with the ubiquitination of proteins associated with the chloroplast envelope during photo-oxidative stress. 25Such ubiquitination may be a mechanism by which photo-damaged chloroplasts are targeted for degradation. 26t first glance, these three mutants appear to use the same 1 O 2 signaling pathway.They all induce PCD and regulate the expression of the same photo-oxidative stress nuclear marker genes.However, it is not known if these mutants represent one or multiple chloroplast signaling pathways.To this end, we recently used a meta-analysis of previously published whole transcriptome data sets of the three mutants to determine if they regulate the same set of genes 27 due to generating the same 1 O 2 signal.We observed that they share a small core transcriptional response to 1 O 2 stress (36 genes), but maintain unique patterns.This result opened the possibility that these mutants use different 1 O 2 signals that report on specific stresses.Next, we combined the suppressor mutations described above with 1 O 2 -producing backgrounds in which they were not originally isolated. 27We then tested the ability of these suppressor mutations to block or alter 1 O 2 signaling in these new genetic backgrounds.Our results suggested that these mutants may represent two distinct 1 O 2 signaling pathways: one represented by flu (involving EX1/EX2 and CRY1), and one represented by fc2 and ch1 (involving PUB4 and OXI1).This was based on the observation that mutations that block signaling in flu (ex1/ex2 and cry1) did not directly block signaling in fc2.The cry1 mutation also did not block signaling in oxi1, while ex1/ex2 were previously shown not to affect 1 O 2 signaling in this mutant. 17In addition, genetic suppressors of fc2 (pub4-6) and ch1 (oxi1) did not affect 1 O 2 signaling in flu.At the same time, fc2 and ch1 seemed to share the same pathway.The pub4-6 mutation was able to block EL-induced PCD in ch1, and the oxi1 mutation was able to block PCD in fc2 adult plants (but not seedlings).Together, these results pointed to chloroplasts using at least two separate 1 O 2 pathways to induce PCD and retrograde signaling.
A fourth, less characterized mutant, accelerated death 2 (acd2), has also been shown to accumulate 1 O 2 , leading to spontaneous lesion formation in adult leaves. 28,29The ACD2 protein is needed to convert red chlorophyll catabolite (RCC) to primary fluorescent chlorophyll catabolite (pFCC) during chlorophyll catabolism. 30In acd2 mutants, the photosensitive tetrapyrrole RCC accumulates, which is likely responsible for the burst of 1 O 2 . 31The site of 1 O 2 production in acd2, however, is not clear.ACD2 is expected to be active near PSII, 32 but also localizes to mitochondria under stress conditions. 33The latter observation may explain why 1 O 2 has been shown to accumulate in acd2 mitochondria. 34Nonetheless, overexpression of ACD2 has been shown to delay the hypersensitive response (HR) induced by Pseudomonas syringae infection, suggesting the regulation of tetrapyrrole catabolism may play a role in a pathogen defense response. 33In citrus, an ACD2 homolog is a target of the Candidatus Liberibacter Asiaticus effector protein SDE15, and this interaction suppresses the plant's hypersensitive response. 35Consequently, ACD2-related 1 O 2 production may act as a mechanism by which plants can trigger PCD in response to pathogen attack.
Previously, it was shown that acd2 mutants do not produce a flu-like signal, as ex1/ex2 and cry1 mutations were unable to block spontaneous cell death phenotypes in acd2. 33To test if fc2 may share a pathway with acd2, we previously generated an acd2 pub4-6 double mutant and showed that it had delayed lesion formation, 27 suggesting that the 1 O 2 produced in acd2 mutants triggers PCD through a PUB4-related mechanism.However, it is unknown if this is the same 1 O 2 pathway also shared with the ch1 mutant.Here, we follow-up on these studies by testing the role OXI1 plays during lesion formation in the acd2 mutant.We show that OXI1 is dispensable for spontaneous lesion formation in acd2, but not for ELinduced 1 O 2 -dependent) lesion formation, suggesting these responses may represent two separate signaling pathways to induce PCD.

Plant material and growth conditions
The wild type (wt) used in this study was Arabidopsis thaliana ecotype Columbia (Col-0).T-DNA line GABI_355H08 (oxi1-1) 36 from the GABI-Kat collection, 37 pub4-6 , 10 and acd2-2 29 were described previously.The line expressing plastid localized YFP (35S::TobaccoRBCS(1-79)-YFP) was described previously. 38dditional information on these lines is listed in Table S1.Double mutants were created by crossing single mutants.Genotypes were confirmed by extracting DNA using a CTABbased protocol 39 and using PCR-based markers to detect the presence of a T-DNA (oxi1) or a SNP (acd2 and pub4-6) as previously described. 27Primer sequences are listed in Table S2.
Seedlings were germinated on half-strength Linsmaier and Skoog medium pH 5.7 (Caisson Laboratories North Logan, UT) in 0.6% micropropagation type-1 agar powder (PlantMedia, CAS:9002-18-0) and grown as previously described. 40Seedlings were first grown in constant light conditions in a Percival Ⓡ model CU-36L5 plant tissue culture chamber (with fluorescent bulbs) with a light intensity of ~ 70 photons µmol photons m −2 sec −1 at 21°C.Seven-day-old seedlings were carefully transferred to soil (PRO-MIX LP15) supplemented with fertilizer (Jack's Classic All Purpose fertilizer, 6.7 mL of 300 g/L solution per flat), and growth was continued in a LED plant growth chamber (Hettich PRC 1700) at ~ 110-120 µmol photons m −2 sec −1 at 21°C and 60% relative humidity, set to diurnal cycling light (16 h light/8 h dark) conditions.Photosynthetically active radiation was measured using a LI-250A light meter with a LI-190 R-BNC-2 Quantum Sensor (LiCOR).

Excess light treatments
21-day-old plants were exposed to EL treatments of 1450-1550 µmol photons m −2 sec −1 white light at 10°C (to offset for excess heat generated by the EL panel) for 24 h in a Percival LED 41L1 chamber (with SB4X All-White SciBrite LED tiles) as previously described. 41The average leaf temperature was measured using an Etekcity Lasergrip 630 Infrared Thermometer and was consistently between 19°C and 20°C.

Confocal microscopy
Leaf sections were imaged on the adaxial side using a Zeiss 880 inverted confocal microscope.The excitation/emissions wavelengths used for chlorophyll autofluorescence, and yellow fluorescent protein (YFP) fluorescence were 633 nm/638-721 nm and 514 nm/519-620 nm, respectively.YFP and chlorophyll were scanned on separate tracks with truncated emissions spectra to prevent signal bleed-over.Images were processed using ZEN BLUE (Zeiss) software and analyzed in IMAGEJ/ FIJI (https://imagej.net).

Measuring reactive oxygen species
1 O 2 was measured with Singlet Oxygen Sensor Green dye (SOSG, Molecular Probes) as previously described. 41Briefly, leaf disks (4 mm) were cut (using a cork borer) from true leaves (#'s 5-6 not containing lesions) and placed in 250 µl of 50 mM phosphate buffer, pH 7.5, wrapped in foil, and returned to the growth chamber for 2 days, which has been shown to be sufficient to detect 1 O 2 in acd2 31 .One hour before light exposure (subjective dawn) on day three, SOSG solution (final concentration 1 μg/μl SOSG solution) was added under dim green light, vacuum infiltrated for 30 min, and incubated for another 30 min.Leaf disks were then returned to the growth chamber and light exposure for 2 h and then imaged.SOSG fluorescence was measured with a Zeiss Axiozoom 16 fluorescent stereo microscope equipped with a Hamamatsu Flash 4.0 camera and a GFP fluorescence filter.The average SOSG signal (fluorescence per mm 2 of each leaf disk was quantified using ImageJ.
H 2 O 2 was measured using 3,3′-diaminobenzidine tetrahydrochloride (DAB) as described. 42Briefly, leaves (# 5-6 not containing lesions) were submerged in DAB solution (1 mg/ml DAB solution + Tween 20 (0.05% v/v)), vacuum infiltrated in the dark, and placed in a tube rotator overnight.The following day, the DAB stain was removed and replaced with a bleaching solution (ethanol:acetic acid:glycerol, 3:1:1).Tubes were then boiled for 15 min, and the bleaching solution was replaced before an overnight incubation.Leaves were imaged and the average DAB signal (fluorescence per mm 2 of each leaf was quantified using ImageJ.

Biomass measurements
Mean dry weight biomass was assessed by collecting total aerial tissue of 57-day-old plants (after seed set) in envelopes.Plant tissue was thoroughly dried for 3 days in a 65°C oven before weighing.

Chlorophyll fluorescence measurements
Chlorophyll fluorescence measurements were conducted with whole plant rosettes as previously described. 40Briefly, the maximum quantum yield of PSII (Fv/Fm) measurements was obtained from whole plant rosettes.Plants were dark acclimated in a FluorCam chamber (Closed FluorCam FC 800-C/ 1010-S, Photon Systems Instruments) for at least 15 min.And measurements were obtained according to the manufacturer's protocol.Individual leaf measurements were extracted from whole plant images.

Results and discussion
Our previous study indicated that 1 O 2 produced in acd2 mutants triggers spontaneous lesion formation and PCD through a PUB4-related mechanism. 27However, it is unknown if this is the same 1 O 2 pathway also shared with the ch1 mutant.To test this, here we generated an acd2 oxi1 double mutant and assessed lesion formation in adult leaves.As shown in Figure 1 (a,b), lesions begin to spontaneously form in acd2 mutants after 21 days in cycling light (16 h light/8 h dark) conditions with 125 µmol photons m −2 sec −1 white light at 21°C.This was particularly evident in older leaves (#'s 3 and 4).As expected, the pub4-6 mutation delayed this lesion formation at least up through 37 days.However, the oxi1 mutation had no discernable effect on this phenotype, and acd2 oxi1 mutants exhibited a similar number of lesions to acd2.We also measured 1 O 2 accumulation in these lines using SOSG (Figure 1(c)).In agreement with previous findings, 31 acd2 mutants overaccelerated 1 O 2 .However, neither pub4-6 or oxi1 mutations had any significant effect on this accumulation, suggesting that pub4-6 was not reducing lesion formation simply by reducing ROS levels.
Next, we tested the effect of the acd2 mutation on photosynthesis by measuring maximum photosynthetic efficiency (F v /F m ) in leaves.As shown in Figure 1(d,e), acd2 mutants begin to exhibit lower F v /F m values after 24 days in older leaves (#'s 3 and 4), but not newer leaves (#'s 5-6 or 7-8), indicating a degree of photosynthetic stress and loss of chloroplast function.This effect was completely reversed by the pub4-6 mutation, but not by the oxi1 mutation.Finally, we tested the final dry weight biomass of these mutants to assess what effect the spontaneous lesions in acd2 have on the final yield.acd2 mutants had significantly reduced final biomass (dry weight) after seed set compared to wt, presumably due to having impaired photosynthesis during the reproductive phase (Figure 1(f)).This was partly reversed by the pub4-6 mutation, but not by the oxi1 mutation.Notably, the pub4-6 mutant did not lead to a general increase in biomass, as shown by the reduced biomass (compared to wt) of the single mutant.Together, this shows that the pub4-6 mutation protects cells and/or chloroplasts to maintain photosynthesis in acd2 mutants, which positively impacts the final biomass yield.The oxi1 mutation, on the other hand, had no measurable effect on any of these phenotypes.Thus, spontaneous lesion formation in acd2 may be distinct from EL-induced 1 O 2 signaling, which involves both PUB4 and OXI1 in wt and ch1 mutants. 12,27o test if this is the case, we grew plants for only 21 days (before we observed spontaneous lesion formation in acd2) and exposed them to EL (1450-1550 µmol photons m −2 sec −1 white light) at 10°C for 6 h or 24 h to induce 1 O 2 and photooxidative stress. 12,17No lesions were detected at 6 h, but as shown in Figure 2(a,b), wt plants started to develop lesions by 24 h.To determine if these lesions correlated with chloroplast rupture, we also exposed wt plants expressing plastidlocalized YFP to EL. Prior to EL, all YFP co-localized with chlorophyll, indicating the expected chloroplast-localization (Figure 2(c)).After 6 h of EL, the distribution of YFP changed markedly in some cells.In these cases, YFP no longer associated with chloroplasts, and was instead distributed throughout the cell, indicating vacuolar collapse and the onset of PCD.YFP-less chloroplasts were also swollen in size (Figure 2(d)), a hallmark of degrading organelles. 11,43After 24, little YFP or chlorophyll was detected, suggesting that chloroplast degradation was complete (Figure 2(c)).Thus, EL stress was able to induce chloroplast degradation reminiscent to 1 O 2 -triggered degradation observed in fc2 , 10 supporting the hypothesis that EL and 1 O 2 induce overlapping pathways. 44,45ext, we tested if our mutants behaved differently in EL.As previously shown, 12,27,41 the pub4-6 and oxi1 mutations delayed EL-induced lesion formation.Unexpectedly, the acd2 mutants also had delayed lesion formation, but the acd2 pub4-6 and acd2 oxi1 double mutants had even fewer lesions (acd2 vs. acd2 pub4-6; p = .008,acd2 vs. acd2 oxi1, p = 0.244 (student's t-tests)).Next, we measured the effect of EL on F v /F m values in whole rosettes.As shown in Figure 2(e,f), 6 h and 24 h of EL reduced F v /F m in wt.As expected, 27 pub4-6 retained slightly higher values at 24 h.Surprisingly, before and after EL, acd2 mutants also had slightly increased F v /F m values compared to wt, indicating an increased tolerance to EL.This tolerance was further increased in the acd2 pub4 and acd2 oxi1 double mutants and the effect was additive (acd2 vs. acd2 pub4-6, p = .016;acd2 vs. acd2 oxi1, p = .001(student's t-tests)).
To test if any plants were experiencing altered photooxidative stress, we measured ROS production.SOSG (the only commercially available in vivo marker specific to 1 O 2 46 is auto-activated under higher light intensities and cannot be used to measure 1 O 2 under EL. 47As such, we decided to measure H 2 O 2 , which is also produced in chloroplasts under EL stress. 48In wt, H 2 O 2 significantly accumulated after 6 h of EL (Figure 2(g,h)).All other tested mutants had similar levels of H 2 O 2 after 6 h, suggesting that none of the mutations delayed lesion formation by limiting ROS production.Interestingly, all lines with the acd2 mutation had significantly higher levels of H 2 O 2 prior to EL stress, compared to wt, which was not significantly changed by 6 h of EL stress.
Together, these EL experiments indicate that EL-induced lesions in 21-day-old plants may be mechanistically distinct to the spontaneous acd2 lesions observed after 24 days, the latter involving 1 O 2 signaling through a unique PUB4-related pathway.Yet, the EL pathway appears to still be active in 21-day-old acd2 mutants as pub4-6 and oxi1 delay EL-induced lesion formation and the drop in Fv/F m values in this mutant.Under EL stress, chloroplasts swell and rupture in a way reminiscent of 1 O 2 -induced chloroplast degradation in fc2 mutants (Figure 2(c,d)), which may involve autophagosomeindependent microauthophagy. 10,11It is unclear if a similar process occurs in acd2 mutants.Further structural studies of chloroplast degradation under different stresses and in different genotypes will be useful in determining if multiple types of degradation machinery can be involved, or if a single type can be induced by different signals.
Notably, acd2 was not sensitive to EL stress, at least before the formation of spontaneous lesions.This was surprising as acd2 potentially accumulates chlorophyll breakdown intermediates near PSII that can produce 1 O 2 , 32 particularly under EL stress.However, such ROS, including the constitutively high levels of H 2 O 2 we observed (Figure 2(g,h)), may lead to a stress-acclimation response leading to reduced EL-sensitivity.Whether such a response involves MBS1, 18 or altered levels of tetrapyrrole intermediates is unknown.
Together, our results further define the 1 O 2 signaling pathways in plants and show that PUB4 and OXI1 represent two partially overlapping pathways in addition to the EX1/CRY1dependent pathway identified in flu mutants (Figure 3).While oxi1 can block 1 O 2 signaling that leads to PCD in fc2 and ch1, pub4-6 can block such signaling in these mutants as well as spontaneous lesions in the acd2 mutant.As acd2 may be producing 1 O 2 to combat pathogens 35 or within mitochondria, 34 it is tempting to conclude that PUB4 may be able to act more broadly in ROS signaling, possibly through immune responses that lead to PCD or hypersensitivity-like responses to pathogens.0][51] and tolerance to heat stress in the dark. 41Such work underlines the complexity of chloroplast signaling, which may indicate how flexible these organelles are in sensing their environments and providing information for the cell.

Figure 1 . 4 Figure 2 .
Figure 1.Assessing the effect of pub4-6 and oxi1 on lesion formation in acd2.(a) Representative images of 24-day-old plants.White arrows indicate lesions.(b) assessment of mean lesion formation (number of rosette leaves with lesions) in plants between 19 and 37 days old (n ≥ 18 plants).(c) singlet oxygen ( 1 O 2 ) accumulation in leaves (#'s 5-6) from 24-day-old plants.Shown are mean singlet oxygen sensor green (SOSG) intensities per leaf disc (n ≥ leaves from individual plants).Below graph are images of representative leaf discs (d) Representative images of 24-day-old plants showing maximum photosynthetic efficiency (F v /F m ) values.(e) mean F v /F m values taken from leaves in panel D. Leaves were separated based on age (#'s 3-4, 5-6, or 6-7), measured, and averaged per plant (n ≥ 3 leaf groups from individual plants).F) mean dry weight biomass (mg) from total aerial tissue of 57-day-old plants (n ≥ 12).All plants were grown in cycling light conditions (16 h light/8 h dark) with 125 µmol photons m −2 sec −1 white light at 21°C.Statistical analyses were performed with a one-way ANOVA.In panel B, a Dunnett's multiple comparisons posttest was used to test variation between genotypes relative to wt at each time point (* = P ≤ .05,** = P ≤ .01,*** = P ≤ .001).In panels C, E, and F, a Tukey's multiple comparisons posttest were used to compare variation between genotypes.Different letters above bars indicate significant differences between genotypes (P ≤ .05).In panel E, separate statistical analyses were performed for the different leaf groups, and the significance for groups #5-6 and #7-8 are indicated by single (ʹ) or double (ʹʹ) prime symbols, respectively.Graph bars indicate ±SEM.Closed circles indicate individual data points.

after 0, 6 ,
or 24 h of EL.Cells with intact (i) and degrading (d) chloroplasts are indicated.Scale bars = 30 μm.(d) mean chloroplast areas from cells with intact or degrading chloroplasts.Areas were estimated based on chlorophyll autofluorescence.Only cells expressing YFP were considered (n ≥ 6 cells from 3 plants).(e) Representative images of stressed plants (immediately after 24 h of EL) showing maximum photosynthetic efficiency (F v /F m ) values.(f) mean F v /F m values calculated from whole plant rosettes after 0 h, 6 h, or 24 h EL exposure (n ≥ 5 plants).(g) shown are representative leaves (#5-6) from plants before and after 6 h EL stress stained with 3,3′-diaminobenzidine tetrahydrochloride (DAB).(h) shown are the mean values of DAB intensity of the leaves in panel G (n = 6 leaves from individual plants).Statistical analyses in panels B, D, F, and H were performed with one-way ANOVAs.In panels B, D, and H, Tukey's multiple comparisons posttest was used to compare variation between genotypes.Different letters above bars indicate significant differences between genotypes (P ≤ .05).In panel H, separate analyses were performed for each time point and the significance for 6 h is indicated by prime (ʹ) symbols.Difference between time points for a genotype were performed by student's t-tests.In panel F, a Dunnett's multiple comparisons posttest was used to test variation between genotypes within a treatment relative to wt. * = P ≤ .05,** = P ≤ .01,*** = P ≤ .001,**** = P ≤ .0001,ns = P ≥ .05.Error bars = ± SEM.Closed circles indicate individual data points.

Figure 3 .
Figure 3. Differential effects on programmed cell death by mutations that block singlet oxygen-signaling.A model summarizing the differential effects on programmed cell death (PCD) by mutations known to block singlet oxygen 1 O 2 )-signaling in Arabidopsis thaliana.Circles in the center row represent four 1 O 2 accumulating mutants and conditions in which 1 O 2 -induced PCD can occur: plastid ferrochelatase 2 (fc2) (green) (diurnal light), chlorina (ch1) (yellow) (excess light), accelerated cell death 2 (acd2) (orange) (spontaneous), and fluorescent in blue light (flu) (blue) (dark-to-light).Circles on the top and bottom rows represent secondary mutations (pub4-6, oxi1, ex1/ex2, cry1) and their ability to block 1 O 2 signaling (PCD) in the seedling (top) and adult stages (bottom).Circles sharing the same color as the 1 O 2 accumulating mutants indicate the mutant background in which these signaling mutants were first discovered.Solid lines and dashed lines indicate direct and indirect suppression of possibly depending on the bulk level of 1 O 2 .Remarkably, these effects CONTACT Jesse D. Woodson jessewoodson@arizona.edu; The School of Plant Sciences, University of Arizona, 303 Forbes Hall, 1140 E. South Campus Drive, Tucson, AZ 85721-0036, USA Supplemental data for this article can be accessed online at https://doi.org/10.1080/15592324.2024.2347783